Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.127802781_127802784del | CA1119039365 | PVT1 | n.202+8047_202+8050del | gnomAD v3 gnomAD v4 |
8 | g.127802783T>A | CA1818529865 | PVT1 | n.202+8049T>A | dbSNP |
8 | g.127802783T>C | CA12821260 | PVT1 | n.202+8049T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.127802783T>G | CA2580596618 | PVT1 | n.202+8049T>G | |
8 | g.127802783T= | CA1818529864 | PVT1 | n.202+8049T= | |
8 | g.127802786_127802787insTACA | CA1119039367 | PVT1 | n.202+8052_202+8053insTACA | gnomAD v3 gnomAD v4 |
8 | g.127802787C= | CA1818529869 | PVT1 | n.202+8053C= | |
8 | g.127802787C>T | CA1818529867 | PVT1 | n.202+8053C>T | dbSNP |
8 | g.127802789del | CA1119039368 | PVT1 | n.202+8055del | gnomAD v3 gnomAD v4 |
8 | g.127802789G>C | CA847202482 | PVT1 | n.202+8055G>C | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802789G= | CA1818529872 | PVT1 | n.202+8055G= | |
8 | g.127802789G>T | CA185785071 | PVT1 | n.202+8055G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.127802791G>A | CA185785072 | PVT1 | n.202+8057G>A | dbSNP |
8 | g.127802791G= | CA1818529874 | PVT1 | n.202+8057G= | |
8 | g.127802791_127802795del | CA1119039369 | PVT1 | n.202+8057_202+8061del | gnomAD v3 gnomAD v4 |
8 | g.127802793G= | CA1818529875 | PVT1 | n.202+8059G= | |
8 | g.127802793G>T | CA847202486 | PVT1 | n.202+8059G>T | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802794G>A | CA185785073 | PVT1 | n.202+8060G>A | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802794G= | CA1818529877 | PVT1 | n.202+8060G= | |
8 | g.127802795_127802810delinsGAGGGAGGCACACTGC | CA1818529879 | PVT1 | n.202+8061_202+8076delinsGAGGGAGGCACACTGC | |
8 | g.127802798_127802812del | CA1818529882 | PVT1 | n.202+8064_202+8078del | dbSNP |
8 | g.127802798_127802799del | CA1119039372 | PVT1 | n.202+8064_202+8065del | gnomAD v3 gnomAD v4 |
8 | g.127802798G>A | CA1818529884 | PVT1 | n.202+8064G>A | dbSNP |
8 | g.127802798G= | CA1818529886 | PVT1 | n.202+8064G= | |
8 | g.127802799G>C | CA847202487 | PVT1 | n.202+8065G>C | dbSNP |
8 | g.127802799G= | CA1818529891 | PVT1 | n.202+8065G= | |
8 | g.127802802G>A | CA185785074 | PVT1 | n.202+8068G>A | dbSNP |
8 | g.127802802G>C | CA1818529896 | PVT1 | n.202+8068G>C | dbSNP |
8 | g.127802802G= | CA1818529897 | PVT1 | n.202+8068G= | |
8 | g.127802803C>A | CA185785075 | PVT1 | n.202+8069C>A | dbSNP |
8 | g.127802803C= | CA1818529901 | PVT1 | n.202+8069C= | |
8 | g.127802806A= | CA1818529905 | PVT1 | n.202+8072A= | |
8 | g.127802806A>G | CA847202491 | PVT1 | n.202+8072A>G | dbSNP |
8 | g.127802809G>A | CA185785076 | PVT1 | n.202+8075G>A | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802809G= | CA1818529907 | PVT1 | n.202+8075G= | |
8 | g.127802811A= | CA1818529909 | PVT1 | n.202+8077A= | |
8 | g.127802812G>A | CA1119039374 | PVT1 | n.202+8078G>A | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802812G= | CA1818529911 | PVT1 | n.202+8078G= | |
8 | g.127802812G>T | CA2542510625 | PVT1 | n.202+8078G>T | |
8 | g.127802812dup | CA1818529912 | PVT1 | n.202+8078dup | dbSNP |
8 | g.127802814_127802815delinsTG | CA1818529913 | PVT1 | n.202+8080_202+8081delinsTG | |
8 | g.127802815del | CA847202494 | PVT1 | n.202+8081del | dbSNP |
8 | g.127802817A= | CA1818529917 | PVT1 | n.202+8083A= | |
8 | g.127802817A>C | CA185785077 | PVT1 | n.202+8083A>C | dbSNP gnomAD v3 gnomAD v4 |
8 | g.127802818_127802819insTTTTAGATTTT | CA2524971332 | PVT1 | n.202+8084_202+8085insTTTTAGATTTT | |
8 | g.127802819C= | CA1818529921 | PVT1 | n.202+8085C= | |
8 | g.127802819C>G | CA1818529923 | PVT1 | n.202+8085C>G | dbSNP |
8 | g.127802820T>C | CA185785078 | PVT1 | n.202+8086T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.127802820T= | CA1818529927 | PVT1 | n.202+8086T= | |
8 | g.127802820_127802821insAGTA | CA2571960798 | PVT1 | n.202+8086_202+8087insAGTA |